JPH0399125A - Cooking utensil - Google Patents

Cooking utensil

Info

Publication number
JPH0399125A
JPH0399125A JP23501989A JP23501989A JPH0399125A JP H0399125 A JPH0399125 A JP H0399125A JP 23501989 A JP23501989 A JP 23501989A JP 23501989 A JP23501989 A JP 23501989A JP H0399125 A JPH0399125 A JP H0399125A
Authority
JP
Japan
Prior art keywords
heater
cooking
fiber
smoke
cooking chamber
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP23501989A
Other languages
Japanese (ja)
Inventor
Akio Fukuda
明雄 福田
Masao Maki
正雄 牧
Yasunori Kaneko
金子 康典
Makiko Waki
脇 真紀子
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP23501989A priority Critical patent/JPH0399125A/en
Publication of JPH0399125A publication Critical patent/JPH0399125A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To indicate clearly the temperature of a heater in a visual sense, increase the brightness of a cooking chamber and clean smoke and stain resultant from cooking by providing a smoke cleaning means based on a catalytic member which uses a flat-shaped silica tube heater and an inorganic fiber porous member and a stain cleaning means based on a coating film. CONSTITUTION:A plurality of heater lines 2 are arranged to run through a flat-shaped silica tube 1 for a cooking utensil, thereby forming a flat-shaped silica tube heater. A reflecting plate 9 is installed near the heater. Furthermore, a catalyzer 3 for smoke treatment is laid out so that an exhaust inlet 4, an exhaust passage 5 and an exhaust outlet 6 may be provided. In addition, an attempt is made to form a film for thermal decomposition of oil stain in an interior 7 of a cooking chamber so that the film may work by the heating operation of a heater 2 or a heater 8 installed on the bottom. After cooling, electric power is supplied to the silica tube heater 2 or the heater 8 for about two hours, which makes it possible to crack oil stain adhering to the interior of the cooking chamber and hence prevents smoke leakage.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は、平面形状の石英管ヒータと煙処理手段と汚れ
を熱分解する手段を備えた調理器に関するものである。
DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a cooking appliance equipped with a planar quartz tube heater, smoke treatment means, and means for thermally decomposing dirt.

従来の技術 従来の調理器に煙処理手段と汚れの熱分解手段とを備え
、かつヒータが平面形状の石英管ヒータを有するものは
みあたらなかった.そして、従来技術では、煙処理手段
は調理器の排気通路に触媒を担持したハニカムを設置し
て油煙などを分解するものが基本的な構威で、ハニカム
以外の触媒体はない。又、汚れの熱分解手段は、調理室
内壁面に耐熱ホーロー被膜を設け調理室内温度を約45
0℃に上げて汚れを分解する方法と、調理室内壁面に触
媒を含む多孔質の被膜を設けホーローの場合より低い温
度で汚れを触媒作用で分解するものである。
PRIOR TECHNOLOGY No conventional cooking appliance has been found that is equipped with a smoke treatment means and a dirt thermal decomposition means, and whose heater is a flat quartz tube heater. In the prior art, the basic structure of the smoke treatment means is to disassemble oil smoke by installing a honeycomb carrying a catalyst in the exhaust passage of the cooking appliance, and there is no catalyst body other than the honeycomb. In addition, as a means for thermally decomposing dirt, a heat-resistant enamel coating is provided on the wall surface of the cooking chamber to reduce the temperature of the cooking chamber to about 45%.
One method is to raise the temperature to 0°C to decompose dirt, and the other is to provide a porous film containing a catalyst on the inner wall of the cooking chamber to decompose dirt using catalytic action at a lower temperature than in the case of enamel.

又、ヒータでは棒状の石英管タイプのヒータ、シーズヒ
ー夕、絶縁性平板にヒータ線を巻いた平面状ヒータがあ
る. 発明が解決しようとする課題 しかしながら、上記従来技術では以下の課題がある.ハ
ニカムを用いた煙処理では、圧力損失の問題で層高が高
くとれない.又はセル数を多くできないことにより処理
能力が低く、煙を完全に分解してしまうには高温化が要
求され、専用ヒータを設けなければならない。
Furthermore, heaters include rod-shaped quartz tube type heaters, sheathed heaters, and flat heaters in which heating wire is wound around an insulating flat plate. Problems to be Solved by the Invention However, the above conventional technology has the following problems. In smoke treatment using honeycomb, a high layer height cannot be achieved due to pressure loss issues. Alternatively, the processing capacity is low due to the inability to increase the number of cells, and a high temperature is required to completely decompose the smoke, and a dedicated heater must be provided.

又、汚れの熱分解では、ホーロー被覆を使うにはヒータ
容量が大きくなってしまい国内100Vでは対応が困難
であり、さらにホーローがヒートショックに弱くクラン
クが発生し剥離する可能性がある。一方、触媒を含む多
孔質被膜の場合は、膜強度が弱くキズ付き易い事と、空
孔内部に分解残査が残り易い事などがある。
In addition, for thermal decomposition of dirt, the use of an enamel coating requires a large heater capacity, which is difficult to handle at 100V in Japan.Furthermore, enamel is susceptible to heat shock and may cause cracking and peeling. On the other hand, in the case of a porous film containing a catalyst, the film has weak strength and is easily scratched, and decomposition residues tend to remain inside the pores.

次に、ヒータでは棒状ヒータの場合には、調理物に焼き
ムラが出易い事、大きな調理室の高温化にはヒータ面積
が小さく熱量不足である事、平面状ヒータの場合には、
ヒータの赤熱状態が見えず視覚的に調理のイメージが得
られない事などがある. 本発明は上記従来技術の課題を解決するもので、従来に
比べて高い煙処理能力と汚れの分解能力を有し、かつ高
温時の赤熱状熊を視覚的に見ることのできる調理器を提
供する. 課題を解決するための手段 上記課題を解決するために本発明は、ヒータ線を少なく
とも2本以上有した平面形状の石英管ヒータと、ヒータ
近傍に酸化触媒を含有した無機繊維多孔体を配置させる
ことによる煙処理手段と、調理室内壁面に汚れの分解除
去能力をもつ被膜を形成し、この被膜上で油汚れ等を熱
分解する手段を調理器に備えるものである。
Next, in the case of a rod-shaped heater, the cooked food tends to be unevenly cooked, the heater area is small and the amount of heat is insufficient for raising the temperature of a large cooking chamber, and in the case of a flat heater,
There are cases where you cannot see the red-hot state of the heater and cannot get a visual image of the cooking process. The present invention solves the above-mentioned problems of the prior art, and provides a cooker that has a higher smoke processing ability and dirt decomposition ability than the conventional one, and can visually see red-hot bears at high temperatures. do. Means for Solving the Problems In order to solve the above problems, the present invention includes a planar quartz tube heater having at least two heater wires, and an inorganic fiber porous body containing an oxidation catalyst arranged near the heater. The cooking appliance is equipped with a means for treating smoke, and a means for forming a film having the ability to decompose and remove dirt on the wall surface of the cooking chamber, and thermally decomposing oil dirt and the like on this film.

作用 以下、本発明の作用について説明する。action Hereinafter, the effects of the present invention will be explained.

まずヒータについて説明する.ヒータは平面状の石英管
と2本以上のヒータ線とから戒る。石英管を平面状にす
ることで加熱面積を広くとることが可能となる.石英管
の温度分布はヒータ近傍が高く、ヒータからずれるにつ
れて低くなるのは明らかである。しかしながら、石英管
は一体である?ので調理室内での赤熱状態が強調されて
視覚上で大きなメリットをもたらす.又、ヒータの温度
立上がりは従来の平面ヒータに比べると早く、広面積で
速熱性がある点が従来に比べ優れている。
First, let's explain about the heater. For heaters, avoid using flat quartz tubes and two or more heater wires. By making the quartz tube flat, it is possible to increase the heating area. It is clear that the temperature distribution of the quartz tube is high near the heater and becomes lower as it moves away from the heater. However, is the quartz tube one piece? Therefore, the red-hot state inside the cooking chamber is emphasized, which brings a great visual benefit. Furthermore, the temperature rise of the heater is faster than that of conventional planar heaters, and it is superior to conventional flat heaters in that it has a wide area and heats up quickly.

次に煙処理手段について説明する. 本発明で用いる酸化触媒はFe,Mn,Cu、Co,N
iなどの遷移金属酸化物(複合酸化物を含む)やPL,
Pdなとの貴金属のいずれでもよい.これらの酸化触媒
を無機繊維多孔体として市販されているS io.−A
lz Os繊維等の不織布に粉末状態で含有させる。S
iO■−AI20.繊維不織布は平均50〜80%の空
隙率(数lO〜数100μmの孔径から戒る)を有して
おり、粒径が約0.1〜10μm程度の煙(油煙等)を
捕捉しやすい。煙が浦捉されると酸化触媒表面には不織
布の構造上、空気中の酸素が容易に供給されており、又
、ヒータ近傍に配置され適当な温度が得られるので、酸
化反応で煙が分解される。以上の事から煙処理に用いる
無機繊維多孔体(不織布)は特にSin.Altos繊
維不織布である必要はなく、Zr0,、Alz Os、
SiCh、SiC、金属、ガラスなど市販されているも
ので適当な空孔と空隙率をもつ不織布あるいは織布であ
ればよい。又、酸化触媒も粉末状態で使用するため表面
積が必ずしも大きくなければならないという事も活性が
高くなければならない事もなく、本発明の煙処理は比較
的簡単な構或で高い性能を引き出すことができる。この
点から、酸化触媒は請求項(4)に挙げられたものでよ
い。
Next, we will explain the smoke processing means. The oxidation catalyst used in the present invention is Fe, Mn, Cu, Co, N
Transition metal oxides (including composite oxides) such as i, PL,
It can be made of any noble metal such as Pd. These oxidation catalysts are commercially available as Sio. -A
It is contained in a powdered state in a nonwoven fabric such as lzOs fiber. S
iO■-AI20. The fibrous nonwoven fabric has a porosity of 50 to 80% on average (pore diameters ranging from several 10 to several 100 μm) and easily captures smoke (oil smoke, etc.) with a particle size of approximately 0.1 to 10 μm. When the smoke is captured, oxygen from the air is easily supplied to the surface of the oxidation catalyst due to the structure of the non-woven fabric, and since it is placed near the heater and an appropriate temperature is obtained, the smoke is decomposed by the oxidation reaction. be done. From the above, the inorganic fiber porous material (nonwoven fabric) used for smoke treatment is particularly suitable for Sin. It does not need to be Altos fiber nonwoven fabric, but Zr0, AlzOs,
Any commercially available nonwoven fabric or woven fabric with suitable pores and porosity, such as SiCh, SiC, metal, and glass, may be used. Furthermore, since the oxidation catalyst is used in powder form, it does not necessarily have to have a large surface area or be highly active, and the smoke treatment of the present invention can achieve high performance with a relatively simple structure. can. In this respect, the oxidation catalyst may be those listed in claim (4).

次に油汚れ等の熱分解について説明する。Next, thermal decomposition of oil stains, etc. will be explained.

調理中に調理室内壁面に付着した油などの汚れは300
℃以上ではタール化し強固に内壁に付着してしまう。上
記の煙処理で用いた触媒体(酸化触媒十無m繊維多孔体
)を使えば簡単に酸化分解しタール化などはないが、上
記触媒体は調理室内壁に適用するほどの強度がない。
Dirt such as oil that adheres to the walls of the cooking chamber during cooking has a rating of 300.
At temperatures above ℃, it turns into tar and firmly adheres to the inner wall. If the catalyst used in the above-mentioned smoke treatment (oxidation catalyst tensless fiber porous material) is used, it will be easily oxidized and decomposed and will not turn into tar, but the catalyst does not have enough strength to be applied to the walls of the cooking chamber.

本発明では、一つの方法としてタール化後の付着強度を
弱めるため、調理室内壁面にMoS2M o O sの
いずれか一方を含む被膜を形戒する。
In the present invention, one method is to form a coating containing either MoS2MoOs on the wall surface of the cooking chamber in order to weaken the adhesion strength after taring.

MoS2 ,Mossは層状の構造を有しており、それ
により被膜表面がすべり性をもつ。すべり性をもつこと
で、被膜上にフイルム状に生戒したタールを容易に剥離
させることが可能となる.調理物から発生する油分は3
50〜400゜Cでは、約lO〜20分でタール化し、
さらに加熱したまま1〜2時間放置するとタールが剥離
し初期の調理室内面にもどすことができる。又、もう一
つの方法としてFe,Mn,Cu,Co,Ni,Moの
ような遷移金属酸化物を含む被膜を形成し、これら酸化
物の酸化作用で汚れを加熱下で分解することできる。
MoS2 and Moss have a layered structure, which makes the coating surface slippery. Due to its slipperiness, it is possible to easily peel off the tar that has been deposited on the coating in the form of a film. The amount of oil generated from cooking is 3
At 50 to 400°C, it turns into tar in about 10 to 20 minutes,
If the tar is left heated for 1 to 2 hours, it will peel off and return to the original surface of the cooking chamber. Another method is to form a film containing transition metal oxides such as Fe, Mn, Cu, Co, Ni, and Mo, and use the oxidizing action of these oxides to decompose the dirt under heat.

実施例 以下、図面を用いて本発明の一実施例を説明する. 第1図は本発明による調理器の一実施例の簡単な断面図
である。平面状石英管1の中にヒータ線2が複数本通さ
れており、平面状石英管ヒータを形成する。このヒータ
の近傍に反射板9を設け、さらに排気人口4、排気通路
5、排気出口6を設けるように煙処理の触媒体3を配置
する。調理室内面7には油汚れ熱分解の被膜を形成し、
上記ヒータ又は底面側に設けられたヒータ8による加熱
で被膜を機能させる。図中10aはドア、10はドアガ
ラス、19は支持脚、20は触媒体の支持板、21は調
理器の外装である。
EXAMPLE An example of the present invention will be described below with reference to the drawings. FIG. 1 is a simplified cross-sectional view of one embodiment of the cooking device according to the invention. A plurality of heater wires 2 are passed through a planar quartz tube 1 to form a planar quartz tube heater. A reflector plate 9 is provided near this heater, and a catalyst body 3 for smoke treatment is arranged so as to further provide an exhaust port 4, an exhaust passage 5, and an exhaust outlet 6. A film of thermal decomposition of oil stains is formed on the inside surface 7 of the cooking chamber.
The coating is made to function by heating with the heater 8 or the heater 8 provided on the bottom side. In the figure, 10a is a door, 10 is a door glass, 19 is a support leg, 20 is a support plate for a catalyst, and 21 is an exterior of a cooking device.

第2図には第1図中の平面状石英管ヒータの簡単な斜視
図を示した. 又、第3図にも他実施例の調理器の断面図を示した。
Figure 2 shows a simple perspective view of the flat quartz tube heater in Figure 1. Further, FIG. 3 also shows a sectional view of a cooking device of another embodiment.

石英管1lの中にヒータ線12が複数本入り平面状石英
管ヒータを形成するが、この場合ヒータ線同士の接触を
避けるため石英管には絞りが施されている.他は第l図
同様に反射板l6、触媒体l3、内面14、ヒータl5
となっている。
A plurality of heater wires 12 are placed inside the quartz tube 1l to form a planar quartz tube heater, but in this case, the quartz tube is constricted to avoid contact between the heater wires. Others are the same as in Figure 1, including a reflecting plate l6, a catalyst body l3, an inner surface 14, and a heater l5.
It becomes.

第4図は第3図中の平面状石英管ヒータの簡単な分解断
面図である。
FIG. 4 is a simple exploded sectional view of the planar quartz tube heater in FIG. 3.

石英管中のヒータ線の本数は第1図、第3図のいずれに
おいても3本として、100v電源で2本あるいは3本
に同時通電した。必要とあれば4本以上にしてもかまわ
ない。通電のパターンをコントロールすればよいことで
ある。
The number of heater wires in the quartz tube was three in both FIG. 1 and FIG. 3, and two or three heater wires were energized at the same time with a 100 V power source. You can use more than four if necessary. All that is required is to control the energization pattern.

第1図、第3図の調理器を用いて約200gのアジを2
匹ずつ焼いた.調理中は、ドアガラス10l7より石英
管ヒータの赤熱状態がわかり、又煙がもれでてくること
もなくアジを焼くことができた。
Using the cooker shown in Figures 1 and 3, prepare approximately 200g of horse mackerel.
I roasted them one by one. During cooking, the red-hot state of the quartz tube heater was visible through the door glass 10l7, and the horse mackerel was grilled without smoke leaking out.

調理後は、石英管ヒータやヒータ8,15に約2時間通
電することで、調理室内面の油汚れを分解できた。又、
この時発生した煙がもれて出てくることもなかった。
After cooking, by energizing the quartz tube heater and heaters 8 and 15 for about 2 hours, the oil stains on the inside of the cooking chamber could be broken down. or,
The smoke generated at this time did not leak out.

以下、平面状石英管ヒータ、煙処理、汚れ熱分解につい
て説明していく。
Below, we will explain the planar quartz tube heater, smoke treatment, and dirt pyrolysis.

まず平面状石英管ヒータであるが、本発明では従来パイ
プ状であった石英管を第2図、第4図よりわかるように
空孔が2次元的広がりをもった形状に加工し、その中に
ヒータ線を複数本挿入したものである。これにより、加
熱面の面積を従来の平面ヒータ並みに大きくすることが
できたために反射板の汚れを防止すると同時にヒータの
赤熱が目でわかるようになった。なおかつ、温度立上が
りは従来の石英ヒータと同様に速いので、本発明による
平面状石英管ヒータは従来の千面ヒータと石英管ヒータ
の長所を合わせもつことができた。
First, regarding the planar quartz tube heater, in the present invention, the conventional pipe-shaped quartz tube is processed into a shape in which the holes are two-dimensionally expanded, as shown in FIGS. 2 and 4. In this case, multiple heater wires are inserted. This allows the area of the heating surface to be made as large as that of conventional flat heaters, which prevents staining of the reflector and at the same time makes it possible to visually see the red heat of the heater. Furthermore, since the temperature rise is as fast as that of the conventional quartz heater, the planar quartz tube heater according to the present invention was able to combine the advantages of the conventional thousand-sided heater and the quartz tube heater.

又、反射板の汚れを防止することで常に高い反射効率が
維持できるので、初期の温度立上がり特性(調理室全体
)の低下を防止できる。
In addition, by preventing the reflector from becoming dirty, a high reflection efficiency can be maintained at all times, so that the initial temperature rise characteristics (for the entire cooking chamber) can be prevented from deteriorating.

次に煙処理であるが、本実施例では無機繊維多孔体とし
て低コストのSin.−AI.Ox繊維の不織布を用い
た。空隙率が約70%の不織布に酸化触媒として1次粒
子径が約0.1μmのFe.O.・CuO−Mnz O
sを約50w t%分散させて触媒体とした。酸化触媒
の配合量は10%以下でも触媒性能が発揮できるようで
ある。不織布の厚さは約1閣とした。この触媒体を第1
図あるいは、第3図の構成で配置すると、調理中の煙は
触媒体表面近傍温度が約350℃位で分解してしまう.
煙の蟹が少ない時は300℃でも分解できることを確認
した。この煙分解に必要な温度は本発明構威のように石
英管ヒータ近傍に触媒体を設けることで十分に得られる
温度であり、第1図において反射板9と触媒体3の距離
は10gm程度が好ましい.この距離が長すぎると触媒
体の温度が低下し、煙浄化は図れない。又、距離が短す
ぎると排気流れに対して圧力損失となるので好ましくな
い。上記の煙処理は従来のハニカムを用いた場合に比べ
、はるかに高い能力を示した.この理由は主に以下の点
である. ハニカムの場合は、焼結体であるため表面近傍だけが反
応の場となり、反応に寄与すると考えられる空隙率や空
孔径が無機繊維多孔体に比べはるかに小さく、その結果
として煙粒子の捕捉、酸素供給の能力が小さくなる。
Next, regarding smoke treatment, in this example, low-cost Sin. -AI. A nonwoven fabric of Ox fibers was used. Fe. O.・CuO-MnzO
A catalyst body was prepared by dispersing approximately 50wt% of s. It appears that the catalytic performance can be exhibited even when the amount of the oxidation catalyst is 10% or less. The thickness of the nonwoven fabric was approximately 1 mm. This catalyst body is
If the arrangement is as shown in Figure 3, the smoke during cooking will decompose when the temperature near the surface of the catalyst is approximately 350°C.
It was confirmed that decomposition can be done even at 300℃ when there are few smoke crabs. The temperature required for this smoke decomposition can be sufficiently obtained by providing a catalyst near the quartz tube heater as in the structure of the present invention, and the distance between the reflector 9 and the catalyst 3 in FIG. 1 is about 10 g. is preferable. If this distance is too long, the temperature of the catalyst will drop, making it impossible to purify the smoke. Moreover, if the distance is too short, pressure loss will occur with respect to the exhaust flow, which is not preferable. The above smoke treatment showed much higher performance than when using conventional honeycomb. The main reasons for this are as follows. In the case of honeycomb, since it is a sintered body, only the area near the surface is the site of reaction, and the porosity and pore diameter, which are thought to contribute to the reaction, are much smaller than those of inorganic fiber porous bodies, and as a result, smoke particles are captured and Oxygen supply capacity becomes smaller.

本発明の触媒体と触媒担持のハニカム(コージェライト
製)の酸化能力の比較のため、5cI1×5CI1の平
板状のテストピースを作威し、各表面にサラダ油0.5
gを滴下して250℃オーブン中に放置したところ、本
発明の触媒体の方は5分以内にサラダ油を酸化分解して
しまった。しかしハニヵムの方は酸化分解は進まず35
0″C以上で60分以上を必要とした。ハニカムに担持
した触媒はベロブス力イト型のL a@.q C eo
1C o 03とPdである。PdはL a*.q C
 ea.+ C O Osの担持層の?から担持した。
In order to compare the oxidation ability of the catalyst body of the present invention and the catalyst-supporting honeycomb (made of cordierite), flat test pieces of 5cI1 x 5CI1 were prepared, and each surface was coated with 0.5% of vegetable oil.
When the catalyst of the present invention oxidized and decomposed the salad oil within 5 minutes, the catalyst body of the present invention oxidized and decomposed the salad oil within 5 minutes. However, in the case of honeycomb, oxidative decomposition does not proceed35
More than 60 minutes was required at a temperature of 0″C or more.The catalyst supported on the honeycomb was a bellows power type L a@.
1C o 03 and Pd. Pd is La*. q C
ea. + C O Os support layer? It was carried from

L a6,w C eo.+ C o Osは、Sin
g  Al■O,繊維不織布に分散すると、250゜C
オーブン中でサラダ油を完全に酸化分解した。
L a6, w C eo. + C o Os is Sin
g Al■O, when dispersed in fibrous nonwoven fabric, 250°C
The salad oil was completely oxidized and decomposed in the oven.

以上のようにSift−AI.03繊維不織布など無機
繊維の多孔体に酸化触媒を分解させたものは高活性の触
媒体が得られ、従来困難であった油煙などの煙処理に最
適である。
As described above, Sift-AI. When an oxidation catalyst is decomposed into a porous body made of inorganic fibers such as 03 fiber nonwoven fabric, a highly active catalyst body can be obtained, and it is ideal for treating smoke such as oil smoke, which has been difficult to do in the past.

次に調理室内壁面の汚れの分解について説明する。Next, the decomposition of dirt on the walls of the cooking chamber will be explained.

汚れの大部分は油分であるが、従来は既に説明したよう
に多孔質の触媒被膜で分解するか熱分解するかのいずれ
かの方法で汚れを分解していた。
Most of the dirt is oil, and conventionally the dirt has been decomposed using either a porous catalytic film or thermal decomposition as described above.

油は、加熱時はカール化し壁面等に強固に付着する.実
施例では、MoS.あるいはMoO1を耐熱性バインダ
のポリボロシロキサンに混合し塗料化した後、被膜を形
成した.塗料には、Moss,MOO3の他にホーロー
フリット、AI.Osを添加した.ポリボロシロキサン
は600゜C以上の熱うなポリボロシロキサン100重
量部に対してMoSよあるいはM o O sを20重
量部、ホーローフリットを20重量部、AI.0.を1
0重量部混合した2種類の塗料を調合した。MoSオ配
合の塗料を塗料1,MoOa配合の塗料を塗料2とした
。塗料lは450℃焼威、塗料2は600″C焼成を行
い、それぞれ第1図に塗料l、第3図に塗料2の被膜を
形成した.この被膜表面を実際の調理で汚した後、ヒー
タ加熱により被膜温度を350゜C以上で約2時間保持
すると調理の汚れは塩分、灰分を除いて全て除去できた
.又、同じ被膜をSUS430のlocmX10cm(
厚さ0.5+am)のテストビース上に形成し、これに
サラダオイル0.5gを滴下した後、約380℃のオー
ブン中に放置したところ、30分以内にフィルム状に固
くタール化し、それ以後徐々にタールが剥離し、約2時
間で完全に剥離した.同様に、ガラス板、金属(SUS
430)板、ホーロー処理した鉄板、従来の多孔質触媒
被膜もサラダオイルの分解テストを行ったが、多孔質触
媒被膜を除いてはタールが付着したままであり、多孔質
被膜でも基材と被膜の界面あるいは空孔の内部にタール
が残査として残っていることがわかった。ここで用いた
多孔質触媒被膜は、リン酸アルごニウム系バインダーに
Mn,CU,Feなど金属の酸化物やケイソウ土、ゼオ
ライト、アルカリ土類酸化物などが含有されているもの
である.又、被膜強度の点で鉛筆硬度は、塗料1、塗料
2によるものでは硬度9H以上となり、ホーローに比べ
ればキズはつきやすいものの、多孔質被膜に比べると格
段に硬く、緻密になっている。さらに、800℃から水
中へのヒートショック10サイクルの後も割れ剥離はな
く、強固な密着であった。
When oil is heated, it curls and adheres firmly to walls, etc. In the example, MoS. Alternatively, MoO1 was mixed with polyborosiloxane, a heat-resistant binder, to form a paint, and then a film was formed. In addition to Moss and MOO3, the paints include enamel frit, AI. Os was added. The polyborosiloxane is a mixture of 20 parts by weight of MoS or MoOs, 20 parts by weight of enamel frit, and 100 parts by weight of polyborosiloxane that is hot at 600°C or higher. 0. 1
Two types of paints were prepared by mixing 0 parts by weight. The paint containing MoOa was designated as paint 1, and the paint containing MoOa was designated as paint 2. Paint 1 was baked at 450°C, and paint 2 was baked at 600''C to form a film of paint 1 in Fig. 1 and paint 2 in Fig. 3, respectively.After the surface of this film was stained by actual cooking, When the coating temperature was maintained at 350°C or higher for about 2 hours by heating with a heater, all cooking stains except salt and ash were removed.Also, the same coating was applied to SUS430 locm x 10cm (
After dropping 0.5 g of salad oil onto the test bead with a thickness of 0.5 + am) and leaving it in an oven at about 380°C, it turned into a hard film-like tar within 30 minutes, and after that, The tar gradually peeled off and was completely peeled off in about 2 hours. Similarly, glass plates, metal (SUS)
430) Plates, enameled iron plates, and conventional porous catalyst coatings were also subjected to salad oil decomposition tests, but tar remained attached to all but the porous catalyst coating, and even with porous coatings, the base material and coating It was found that tar remained as a residue at the interface or inside the pores. The porous catalyst film used here contains oxides of metals such as Mn, CU, and Fe, diatomaceous earth, zeolite, and alkaline earth oxides in an argonium phosphate binder. In addition, in terms of film strength, the pencil hardness of Paint 1 and Paint 2 is 9H or higher, and although it is more easily scratched than enamel, it is much harder and denser than a porous film. Further, even after 10 cycles of heat shock from 800° C. to water, there was no cracking or peeling, and strong adhesion was observed.

本発明の被膜は、潤滑剤として用いられているMob.
の滑りの特性を生かしたものであり、MoO3でも似た
ような結果が得られたので、第1図と第3図の被膜とし
て応用した。化合物の構造上、層状であるという共通点
で、他にモンモリ口ナイト等のシリケート化合物を塗料
中に混合してみたが、サラダオイル分解では好ましい結
果は得も塗料中にl昆合してみたが、これも、サラダオ
イル分解には不適であった。よって、MoSz  M0
0=力{適当であることがわかる。
The coating of the present invention is applied to Mob., which is used as a lubricant.
Since similar results were obtained with MoO3, it was applied as the coatings shown in Figures 1 and 3. We also tried mixing other silicate compounds such as montmori kuchinite into the paint due to the common feature that the compounds are layered in structure, but we did not get favorable results when decomposing salad oil. However, this was also unsuitable for decomposing salad oil. Therefore, MoSz M0
0=Force {It can be seen that it is appropriate.

一方、MOS2.MO○,以外に酸化活性を有するFe
,Mn,Cu,Co,Ni,Moの酸化物を含む被膜も
作威した。バインダはポリボロシロキサンとし、バイン
ダ100重量部に対し、酸化物を30重量部、ホーロー
フリットを20重量部、AL20,をlO重量部配合し
た。これを、前記StlS430テストピース上に60
0゜C焼成で被膜形成した。用いた酸化物は、Fe2 
0z  ・Mnz 03  ・Cu○,NiO−MoO
i ,Cot Os  ・Mnz o3  ・cuO,
Cent H CuXMns−x Oa  (0<x<
1.5)である.汚れ分解テストとしてテストピース被
膜上にサラダオイルを0.5g滴下し350”C,38
0゜C,  400’Cのオープン中で放置したところ
、38(1℃では2〜3時間で分解したが、350’C
では分解できなかった。この結果から、遷移金属酸化物
を含む被膜も本発明に適用できることがわかる。
On the other hand, MOS2. Fe with oxidizing activity other than MO○
Coatings containing oxides of , Mn, Cu, Co, Ni, and Mo were also produced. The binder was polyborosiloxane, and to 100 parts by weight of the binder, 30 parts by weight of oxide, 20 parts by weight of hollow frit, and 10 parts by weight of AL20 were blended. Apply this on the StlS430 test piece for 60 minutes.
A film was formed by firing at 0°C. The oxide used was Fe2
0z ・Mnz 03 ・Cu○, NiO-MoO
i , CotOs ・Mnz o3 ・cuO,
Cent H CuXMns-x Oa (0<x<
1.5). As a dirt decomposition test, 0.5g of salad oil was dropped onto the test piece film at 350"C, 38
When left in an open air at 0°C and 400'C, 38% (decomposed in 2 to 3 hours at 1°C, but at 350'C
I couldn't disassemble it. This result shows that films containing transition metal oxides can also be applied to the present invention.

又、バインダはポリポロシロキザンの他に構造がWIi
91しているポリチタノ力ルポシランでもよい。
In addition to polyporosiloxane, the binder has a structure of WIi.
91 polytitanoloposilane may also be used.

ポリチタノカルボシランの場合、ポリボロシロキサンに
比べ光沢のある被膜が得られる事が多い。
In the case of polytitanocarbosilane, a glossier coating can often be obtained than polyborosiloxane.

発明の効果 以上説明してきたように本発明の調理器は、今までにな
い平面状の石英管ヒータを備え、無機繊維多孔体を用い
た触媒体による煙浄化手段と、MO32あるいはMoO
sを含有する被膜による汚れ浄化手段も備えているので
、 (1)  ヒータを使っての加熱調−理時に、ヒータの
温感が視覚的に分かり、又調理室内の明るさも従来に比
べ明るくすることができる。
Effects of the Invention As explained above, the cooking appliance of the present invention is equipped with an unprecedented planar quartz tube heater, smoke purification means using a catalyst body using an inorganic fiber porous body, and MO32 or MoO
(1) When cooking using a heater, you can visually feel the warmth of the heater, and the brightness inside the cooking chamber is also brighter than before. be able to.

(2)調理による煙、汚れを浄化できるので、クリーン
な調理が可能となる。
(2) Clean cooking is possible because smoke and dirt from cooking can be purified.

【図面の簡単な説明】 第1図は本発明の一実施例の調理器の概略の断面図、第
2図は第1図の調理器で用いた平面状石英管ヒータの概
略の分解断面図、第3図は同他の実施例の調理器の概略
の断面図、第4図は第3図の調理器で用いた平面状石英
管ヒータの概略の分解断面図である。 1・・・・・・平面状石英管、2・・・・・・ヒータ線
、3・・・・・・触媒体、5・・・・・・徘気通路、7
・・・・・・被膜形成した調理室内面、loa・・・・
・・ドア。
[Brief Description of the Drawings] Fig. 1 is a schematic cross-sectional view of a cooking device according to an embodiment of the present invention, and Fig. 2 is a schematic exploded cross-sectional view of a flat quartz tube heater used in the cooking device of Fig. 1. , FIG. 3 is a schematic sectional view of a cooking device of another embodiment, and FIG. 4 is a schematic exploded sectional view of a planar quartz tube heater used in the cooking device of FIG. 3. DESCRIPTION OF SYMBOLS 1... Planar quartz tube, 2... Heater wire, 3... Catalyst body, 5... Wandering passage, 7
...Inner surface of the cooking chamber with film formed, loa...
··door.

Claims (5)

【特許請求の範囲】[Claims] (1)調理物を加熱するための調理室と、調理室内部が
見える透光性のドアと、調理物を加熱するためのヒータ
と、調理物を調理中に発生する煙処理手段と、調理室内
壁に付着した油等の汚れを熱分解する手段とを備え、前
記ヒータはヒータ線を少なくとも2本以上有した平面形
状の石英管ヒータであり、前記煙処理手段は、前記ヒー
タ近傍の高温部分にヒータと一定距離をおいて相対して
酸化触媒を分散した無機繊維の多孔体から成る触媒体を
設け、かつ前記ヒータと触媒体の間の一定距離の空間を
排気通路とし、前記汚れを熱分解する手段は、前記調理
室内面に汚れを分解除去する能力を有する被膜を形成し
た調理器。
(1) A cooking chamber for heating food, a translucent door through which the inside of the cooking chamber can be seen, a heater for heating food, a smoke disposal means generated during cooking, and a cooking chamber. The heater is a planar quartz tube heater having at least two heater wires, and the smoke processing means is a means for thermally decomposing dirt such as oil adhering to the indoor wall. A catalyst body made of a porous inorganic fiber in which an oxidation catalyst is dispersed is provided at a certain distance from the heater, and a space at a certain distance between the heater and the catalyst body is used as an exhaust passage to remove the dirt. The thermal decomposition means is a cooking appliance in which a coating having the ability to decompose and remove dirt is formed on the inside of the cooking chamber.
(2)汚れを分解除去する能力を有する被膜が、ポリボ
ロシロキサンあるいはポリボロチタノカルボシランをバ
インダとし、これに少なくともMoS_2あるいはMo
O_3のいずれかを主成分とするフィラーを分散したも
のである請求項(1)記載の調理器。
(2) The coating that has the ability to decompose and remove dirt uses polyborosiloxane or polyborotitanocarbosilane as a binder, and at least MoS_2 or Mo
The cooking device according to claim 1, wherein a filler containing any one of O_3 as a main component is dispersed.
(3)汚れを分解除去する能力を有する被膜が、ポリボ
ロシロキサンあるいはポリチタノカルボシランをバイン
ダとして、少なくともMn、Cu、Co、Ni、Moの
うちいずれか一種以上の酸化物を分散したものである請
求項(1)記載の調理器。
(3) A film that has the ability to decompose and remove dirt, using polyborosiloxane or polytitanocarbosilane as a binder, and dispersing at least one or more oxides of Mn, Cu, Co, Ni, and Mo. The cooking device according to claim (1).
(4)酸化触媒が、遷移金属の酸化物あるいは複合酸化
物、遷移金属と他元素の複合酸化物、白金族元素、遷移
金属のいずれか一種以上である請求項(1)記載の調理
器。
(4) The cooking device according to claim (1), wherein the oxidation catalyst is one or more of the following: an oxide or composite oxide of a transition metal, a composite oxide of a transition metal and another element, a platinum group element, or a transition metal.
(5)無機繊維の多孔体が、SiO_2−Al_2O_
3繊維、SiO_2繊維、ガラス繊維、金属繊維、Al
_2O_3繊維、ZrO_2繊維、SiC繊維のうちい
ずれかの不織布あるいは織布である請求項(1)記載の
調理器。
(5) The porous body of inorganic fiber is SiO_2-Al_2O_
3 fiber, SiO_2 fiber, glass fiber, metal fiber, Al
The cooking appliance according to claim (1), which is a nonwoven fabric or a woven fabric of any one of _2O_3 fiber, ZrO_2 fiber, and SiC fiber.
JP23501989A 1989-09-11 1989-09-11 Cooking utensil Pending JPH0399125A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP23501989A JPH0399125A (en) 1989-09-11 1989-09-11 Cooking utensil

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP23501989A JPH0399125A (en) 1989-09-11 1989-09-11 Cooking utensil

Publications (1)

Publication Number Publication Date
JPH0399125A true JPH0399125A (en) 1991-04-24

Family

ID=16979873

Family Applications (1)

Application Number Title Priority Date Filing Date
JP23501989A Pending JPH0399125A (en) 1989-09-11 1989-09-11 Cooking utensil

Country Status (1)

Country Link
JP (1) JPH0399125A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0517406U (en) * 1991-08-01 1993-03-05 三洋電機株式会社 Heating cooker
US7554060B2 (en) 2006-09-29 2009-06-30 England Raymond O Displaying cooking-related information
JP2012187417A (en) * 2012-05-17 2012-10-04 Mitsubishi Electric Corp Cooker

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0517406U (en) * 1991-08-01 1993-03-05 三洋電機株式会社 Heating cooker
US7554060B2 (en) 2006-09-29 2009-06-30 England Raymond O Displaying cooking-related information
JP2012187417A (en) * 2012-05-17 2012-10-04 Mitsubishi Electric Corp Cooker

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